Artificial intelligence-driven integration of single-cell RNA sequencing and transcriptome analysis to decipher

Ni Li1, Jinquan Lin2,3, Chunyu Wang3

  • 1Health Management Center, People's Hospital of Guilin, Guilin, 541002, Guangxi, China.

Discover Oncology
|March 14, 2025
PubMed
Abstract

Insights

Artificial intelligence identified apolipoprotein E (APOE) as a key driver of immunosuppression in gastric cancer (GC). APOE promotes tumor progression by polarizing M2 macrophages, highlighting its potential as a prognostic marker and therapeutic target for GC.

Area of Science:

  • Oncology
  • Immunology
  • Bioinformatics

Background:

  • Gastric cancer (GC) presents a significant global health burden with high mortality and limited diagnostic tools.
  • Tumor heterogeneity complicates effective GC treatment, demanding advanced analytical approaches.
  • Artificial intelligence (AI) shows promise in dissecting complex cellular dynamics and gene regulatory networks in cancer.

Purpose of the Study:

  • To explore the tumor microenvironment in GC using AI-enhanced single-cell RNA sequencing (scRNA-seq).
  • To identify novel prognostic markers and therapeutic targets within the GC tumor microenvironment.
  • To elucidate the role of specific genes, particularly apolipoprotein E (APOE), in GC progression and immune evasion.

Main Methods:

  • Analysis of scRNA-seq and transcriptome data from GC patients using AI-driven methodologies.
  • Identification and characterization of macrophage subsets within the GC tumor microenvironment.
  • High-variance gene screening to pinpoint hub genes, followed by experimental validation of APOE expression and function in GC cell lines.

Main Results:

  • AI-enabled analyses confirmed the immunosuppressive function of APOE in gastric cancer.
  • APOE was identified to induce immunosuppression via M2 macrophage polarization, promoting tumor progression.
  • An immune-related survival model was developed, demonstrating APOE's association with poorer patient prognosis and predicting immunotherapy response.

Conclusions:

  • AI-driven approaches effectively elucidate the role of APOE in GC pathogenesis.
  • APOE's regulation of M2 macrophages establishes it as a valuable prognostic biomarker.
  • Targeting APOE offers a potential therapeutic strategy for precision medicine in gastric cancer management.

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